Robertson Francis P, Goswami Rup, Wright Graham P, Imber Charles, Sharma Dinesh, Malago Massimo, Fuller Barry J, Davidson Brian R
Division of Surgery and Intervention Science, Royal Free Campus, University College London, Pond Street, NW3 2QG, UK.
Department of Hepatico Pancreatico Biliary Surgery and Liver Transplantation, Royal Free Hospital Foundation Trust, Pond Street, NW3 2QG, UK.
HPB (Oxford). 2017 Sep;19(9):757-767. doi: 10.1016/j.hpb.2017.05.005. Epub 2017 Jun 24.
Ischaemia Reperfusion (IR) injury is a major cause of morbidity, mortality and graft loss following Orthotopic Liver Transplantation (OLT). Utilising marginal grafts, which are more susceptible to IR injury, makes this a key research goal. Remote Ischaemic Preconditioning (RIPC) has been shown to ameliorate hepatic IR injury in experimental models. Whether RIPC can reduce IR injury in human liver transplant recipients is unknown.
Forty patients undergoing liver transplantation were randomized to RIPC or a sham. RIPC was induced through three 5 min cycles of alternate ischaemia and reperfusion of the left leg prior to surgery. Data on clinical outcomes was collected prospectively. Per-operative cytokine levels were measured.
Fourty five of 51 patients approached (88%) were willing to enroll in the study. Five patients were excluded and 40 randomized, of which 20 underwent RIPC which was successfully completed in all patients. There were no complications following RIPC. Median day 3 AST levels were slightly higher in the RIPC group (221 IU vs 149 IU, p = 1.00).
RIPC is acceptable and safe in liver transplant recipients. This study has not demonstrated evidence of a reduction in short-term measures of IR injury. Longer follow up will be required and consideration of an altered protocol.
缺血再灌注(IR)损伤是原位肝移植(OLT)后发病、死亡和移植物丢失的主要原因。使用对IR损伤更敏感的边缘供肝,使这成为一个关键的研究目标。远程缺血预处理(RIPC)已被证明可改善实验模型中的肝脏IR损伤。RIPC是否能减少人类肝移植受者的IR损伤尚不清楚。
40例接受肝移植的患者被随机分为RIPC组或假手术组。在手术前通过对左腿进行三个5分钟的交替缺血和再灌注周期诱导RIPC。前瞻性收集临床结局数据。测量术中细胞因子水平。
纳入研究的51例患者中有45例(88%)愿意参加。5例患者被排除,40例被随机分组,其中20例接受RIPC,所有患者均成功完成。RIPC后无并发症发生。RIPC组第3天AST水平中位数略高(221 IU对149 IU,p = 1.00)。
RIPC在肝移植受者中是可接受且安全的。本研究未证明有证据表明IR损伤的短期指标有所降低。需要更长时间的随访并考虑改变方案。